Re: [Biofuel] Oooops! to much acid

2006-01-09 Thread Keith Addison
  Thanks Keith,

You're welcome Mick.

As it turns out, between posting this message and receiving your reply I
did some thinking and came up with the same solution.
I've washed this batch twice since and the PH is coming up slowly,
currently about PH 6.5. Tap water here is about PH 7.6 so I estimate
another two or three washes will do it, maybe. Lots of water unfortunately
however I suppose it can't be avoided.

Keep it for future washes? - 3rd wash water for the next 2nd wash etc.

Not good considering Sydney is on
level 3 water restrictions caused no doubt by the urban sprawl, drought
conditions and infrastructure not keeping pace.
I was thinking, is it possible to speed this process up and reduce the
water used by using someting like Bi-carb Soda in the wash water to
neutralise the acid further? Or would this complicate things?

I really don't know, but are you trying to neutralise the acid or to 
get rid of it? Maybe it would be faster but maybe you might end up 
with some neutralised acid and some equally neutralised Bi-carb Soda 
both still in the fuel. But I don't know. I'd stick with the washing 
I guess, you should have enough time.

I'm hoping I can manage to do the necessary washes and dry the fuel before
I hit the road at the end of the week.

Thanks again Keith for your advise, much appreciated.

HIH Mick, hope it works out too, have a good trip.

Best

Keith


Mick

Hello Mick
 
 Hi Guys.
  I was hoping this day would never come.
  
  I’ve been making Bio from WVO for over 12 months now with great success
  using the standard Base catalyst method.
  
  I run it in my 1992 80 series Toyota Land Cruiser with about 340,000 Km
  on
  the clock and she purrs like a Kitten.
  
  I find the web site an excellent wealth of knowledge and a great place
  to
  learn the different theories and ideas from other like minded soles.
  Up until now reading and re reading this info has been of great
  assistance
  to me when in doubt/trouble, however this time I’ve ended up with 180
  liters of Bio with a PH of  5.8. after stuffing up the calculations
  with
  the acid quench in the wash water.
  
  I now find myself with a self induced problem with this latest batch
  and I
  would like to ask the mailing list for advice so I can go on my annual
  camping trip and not have to pay $1.30/Litre at the pump here in
  Sydney.
 
 I have done a tritation of the washed bio and it gave me a 0.075
  tritation
 as per the 'Better tritation method. I'm concerned that I have converted
 some of the Bio back to FFA's.
 
  If the pH is below 7 then you'll get a positive titration reading,
  but I don't see the point of titrating it. If you have converted
  biodiesel back to FFA it sure won't be much. The low-ish pH reading
  is much more likely to be due to residues of the acid you used in the
  wash quench. It can take quite a lot of qwashing to get it out. Keep
  on washing it until the pH returns to something near neutral (or the
  same as your wash water).
 
 My questions are:-
  A. Is this enough catalist to neutralize the acid?
  B. If so how much Methanol should I use for the reaction?
  C. Is this the best method to bring this batch back to PH 7?
 
  You're planning to neutralise the excess acid you used in the wash
  quench by re-processing the biodiesel? Overkill, just wash it some
  more, maybe quite a lot more. If that doesn't work then we can think
  again.
 
  Best
 
  Keith
 
 
  
  Thanks
  Mick Ellis


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Re: [Biofuel] Acid - Base questions

2006-01-09 Thread Keith Addison
Hi Ken

On Jan 8, 2006, at 2:15 AM, Jan Warnqvist wrote:

 
  I was referring to acid esterification of FFA:s / oil without passing
  through the soap step. These reactions are often incomplete, and
  moreover, quite slow.


Not only that, but difficult to isolate your biodiesel from the react-
ants.

After the acid step? No need.

My experience with straight esterification is that you always
have two phases, but you can't ever tell what's in each phase.
It starts out, of course, with alcohol in one and FFA in the other.
After the reaction has gone as far it's going to (many hours of agit-
ation at high temps),

Well, if you like. Or perhaps not many hours at not very high temps.

there's a combination of biodiesel, FFA, acid,
and a little methanol in the oily phase, and the huge excess of meth-
anol plus water and most of the acid in the aqueous phase. Hard to
ever get pure biodiesel, or even know how far the reaction has gone,
and you can't easily purify or wash the biodiesel without reversing
the reaction to some extent.

Huh? Easy washing, high-quality product, no reverse reaction. After 
completing the second-stage base transesterification step that is, I 
guess that's what you mean.

I'm sure it's doable, once you work out all the variables and have a
process down with good testing of your product. For me, the base-
catalyzed reaction is much more practical.

To each his own, of course. For me, single-stage base is primitive by 
comparison with acid-base, and I'm not at all alone in thinking that.

Just had yet another newbie doing the Foolproof method, as-is, this 
one another school student doing it for his science fair. It works 
great, thanks! We tell them don't do it, start at the beginning, 
learn the whole thing so you can do troubleshooting, but a lot of 
people jump in anyway and most of them don't seem to have any 
problems. We get a lot of feedback on it, what I said about it the 
other day has a firm basis:

You try the Foolproof method and sometimes people don't have any 
success with it and maybe come back later and try again, but most 
likely it works just fine, or you have to fiddle with it a bit and 
then it works just fine, or maybe you have to fiddle with it quite a 
lot, and then it works just fine. (I didn't have to fiddle with it, 
it worked just fine, but I fiddled with it anyway and now it works 
even finer.)

Just as an aside, I know you didn't say that, but IMHO it's not a 
good approach to view the acid-base process as a normal single-stage 
base transesterification with an add-on in front. When the acid step 
is done and you start the base transesterification step you're not 
starting from the same place as you would be if you were doing a 
simple single-stage base reaction with lower-FFA oil. There are some 
very complicated ways to proceed, and some very easy ways too. 
Titrating it for instance might not tell you much, or might not tell 
you what you think it's telling you (though it might work anyway). 
Best approach it as a single integrated process with two steps. Sorry 
to be so vague, perforce, but it's a good hint. Aleks's Foolproof 
method is definitely the place to start with acid-base and maybe to 
stay with, which most people seem to do.

Regards

Keith



-K


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[Biofuel] Venezuela's diesel in Chicago - blog

2006-01-09 Thread doug
http://newstandardnews.net/alivewires/business/content/?show_item=2729


  Venezuelan Fuel Story Leads to Action in Chicago

POSTED BY: *Brian Dominick* 
http://newstandardnews.net/content/?action=show_contributor_biocontributorID=1
 

BLOGGING: Chicago Turns Down Discounted Venezuelan Oil 
http://newstandardnews.net/content/?action=show_itemitemid=2710

The following is an excerpt from an email sent to The NewStandard by 
Chicago media activist and long-time TNS reader/supporter Mitchell 
Szczepanczyk about the impact of the story we ran last week by Jessica 
Pupovac. The story concerned the Chicago Transit Authority's decision to 
decline an offer of discounted diesel for its buses from 
Venezuelan-owned Citgo oil, the only condition being they had to pass 
the savings on to poor public-transit users.

Within a day of the post of Jessica's story on TNS, it got
reposted/linked on two widely-read Chicago-area websites: Chicago
Indymedia
http://chicago.indymedia.org/newswire/display/67794/index.php
(which prominently re-featured http://www.chicago.indymedia.org/
the story) and Gapers Block
http://www.gapersblock.com/news/archives/2005/12/#011709. Another
blog, Chicagoist

http://www.chicagoist.com/archives/2005/12/30/new_years_resolution_for_cta_hire_competent_people.php,
also linked to the story.

It continued spreading among a variety of left-of-center websites:
COANews

http://www.coanews.org/tiki-read_article.php?articleId=539PHPSESSID=41772ca6c1f1954e0dbbcd39a533bbef
posted it as their lead story, Alternet
http://www.alternet.org/story/30296/ reprinted the story in its
entirety and featured it.

Then yesterday, things really got big. A number of prominent
Chicago-area legislators held a press conference about the matter.
Somehow they heard about the story and vented loudly. The coverage
of that press conference and the story led to stories in the
/Chicago Sun-Times
http://www.suntimes.com/output/news/cst-nws-citgo05.html/, the
/Chicago Tribune

http://www.chicagotribune.com/business/chi-0601050105jan05,1,4069803.story?coll=chi-business-hed/
(despite a previous unsuccessful attempt on my part to get the
Tribune interested in the story), and on Chicago's CBS radio
affilate http://www.wbbm780.com/pages/1776.php and Chicago Public
Radio

http://www.publicbroadcasting.net/chicago/news.newsmain?action=articleARTICLE_ID=861492.
 

TNS was cited /immediately/ by Chicago-area legislator Luis
Guttierez's communications director as a key source for the story
getting reposted across the web and onto wider public consciousness,
continuing to add to the considerable value of TNS.

We don't usually have time in our day to do this level of follow-up on 
any particular story we publish, but it's really gratifying when a 
reader contacts us to let us know what a difference our journalists make.

-- 
All generalizations are false.  Including this one.

* * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * * *

This email is constructed entirely with OpenSource Software.
No Microsoft databits have been incorporated herein.
All existing databits have been constructed from recycled databits. 


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Re: [Biofuel] Dewatering with vacuum.

2006-01-09 Thread Joe Street




Hey Logan and David;

These numbers are reasonable. (don't forget to factor in an amount for
a steady state leake rate on your system as this adds to the load your
pump will see as it approaches base vacuum) Actually I can get on the
order of 100 to 200 ml water out of 25 liters of oil at times
collecting in my liquid trap. This is estimated I have not measured
it. Perhaps I should. But this is after heating to 55 degrees celsius
and draining any liquid water that precipitates. So 200 mls in 25
liters is 0.8% water by volume. I'm not sure what your batch size is
but as a conservative figure use 1% to figure the amount of water you
will have to remove by vacuum. Also remember that a 5 CFM pump will
not necessarily give you 5 CFM as was pointed out before. And even
after correcting it using gas law equation it still is hampered by
conductance of piping between the pump and chamber. Rule of thumb here
is use large diameter pipe (as large as the pump inlet if possible) and
as few elbows as possible will help a lot.
To give you a feel for these factors consider my system takes about an
hour to remove said amount of water. My system is relatively leak
tight I can get to 29 inches ultimate on a dry system, so I am getting
an EFFECTIVE throughput of about 4 to 5 liters per minute at vacuum BUT
I am using a dual stage rotary pump which is designed to do 18 CFM.
Throughput is reduced dramatically by the fact that I am pumping
through a 1/4" tube!! Bear in mind that from the standpoint of
throughput bigger is always better, but as a girl I once knew taught
me; quality counts for more. When I was pumping through 1/2" copper
pipe I only succeeded in causing the contents of the reactor to froth
up and " boil over" contaminating the liquid trap in the process. So
it is possible to have too much of a good thing. You can reduce the
conductance of the piping or install a valve for throttling the pump to
avoid this problem and toward the end of the drying cycle open up the
valve to speed up the end game. If your reactor starts rumbling and
dancing around on it's stand it is a good bet that you will suck liquid
up into the condenser, especially if the reactor is filled to a high
level.
I hope I have helped and not made it seem a lot more complicated. If
so take a hint from the fact that my pump is more than adequate for my
30 liter size reactor. I get a sense that it could easily handle a 150
liter tank. There is a tradeoff between heat and vacuum. Either one
can speed the drying process but you don't want froth! When I started
learning about vacuum my mentor said " you can't rush a vacuum son - we
got time for a coffee" so true.

Cheers
Joe



logan vilas wrote:

  David

Sorry if that number's wrong it's what I've been told from the only person I 
know who does AC work.

But that number makes it sound a lot better. You will not have 1 cubic foot 
of water in your oil after you settle and drain it. If you do then you need 
to get a better method. There is likely less then 1 cubic inch after 
setteling and draining. That would only take 6 miniutes to remove.

Logan Vilas

- Original Message - 
From: "David Miller" [EMAIL PROTECTED]
To: Biofuel@sustainablelists.org
Sent: Friday, January 06, 2006 1:13 PM
Subject: Re: [Biofuel] Dewatering with vacuum.


  
  
logan vilas wrote:



  Water boils off at 43F at 20-50mmhg of vacuum at sea level. At 140F it
takes about 150-200mmhg. When fluids are mixed togther the Pressure of
Vaporization changes especially when thouroughly mixed. You do not
need a condensor if you are useing a AC type vacuum pump(that's what
they are designed for).

I know iowa's BECON program flash heats their oil to 230F then runs it
through a vacuum chamber to achieve dewatering. Unless you have a very
large vacuum pump or very little water in your oil it will take a long
time. Water multiplies in volume by 10-18 thousand times when boiled.
  


Say WHAT?  I'm not sure what number you mean by "10-18 thousand".  The
number I remember is about 1700 times.



  1 Cubic foot =  1728 cubic inches
1 Cubic Inch of water when boiled off = 5.79 cubic feet minimum
1 gallon = 231 cubic inches

Vacuum Distilation alone would take a huge amount of time. I would
still heat then let it settle and remove the water off the bottom.
Then use vacuum distilation. Remember if you buy a 5CFM vacuum pump
that is displacement of the piston at no load and full rpm. When you
start pulling a vacuum that number falls off quickely and at 30" that
is probably less then 1CFM.
  


You have to multiply the CFM by the pressure. 1/30 atmosphere * 5 CFM =
1/6 CFM.  It you're trying to pump off a cubic foot of water it would
take something like 1700 * 6 minutes.  That's a long time to wait:)

--- David

  
  

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Re: [Biofuel] Chicage - Venezuela

2006-01-09 Thread Joe Street
But this whole discussion is somewhat academic isn't it?  I mean surely 
to blazes the city of Chicago must already be involved in international 
terrorism?  I mean when you consider that the US administration is one 
of the worst offenders in that regard, I can't imagine that a city the 
size of Chicago can plead innocence on the charge.  There must be 
military contractors in the area and in the very least the city is 
making tax revenues off of thier operations within the municipality 
which means the city is already complicit in acts of terror and 
agression all over the world! Oh wait - I forgot we don't tax the rich 
and powerful - nev'r mind.

Joe

Mike Weaver wrote:

But we seem to have no problem buying oil from Saudi Arabia, which has 
had far more to do with funding and sponsoring terrorism than
Venezuela.  I have yet to see anything conclusive about Chavez other 
than he has clamped down on some members of the opposition in his own 
country.
I fail to see how he is much of a threat to the US.

Not to mention, there is a Citgo station AT THE PENTAGON!  It sells 
Biodiesel!

My head hurts.

Mike

Aramco is a foreign government-owned company, are your local governments 
allowed to buy fuel?

Anyway, whatever, the news report says:

  But two months later, despite claims of a looming budget crisis, the
  CTA president has no intent or plan to accept the offer, according
  to CTA spokesperson Ibis Antongiorgi. She gave no explanation.

If your explanation had any chance of standing up I don't doubt she'd 
have used it, but she didn't. People like Weisbrot would surely know it 
too. I think you're just grabbing for an excuse.

IMHO, considering the current context in the US of oil interests, 
corruption and interfering with foreign governments (and even your own), 
your arguments seem somewhat bizarre. In the context of the poor too, 
especially after some of Hurricane Katrina's revelations.
But you blamed the victims at the time, didn't you?

Nobody's said the S-word yet (aarghh), LOL!

Best

Keith



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Re: [Biofuel] Biodiesel Testing excessive methanol

2006-01-09 Thread Joe Street




If the bio was unwashed (as you state below) then how could it have
given good results in the methanol test as stated by Jan below, below?
I find that the methanol test is quite stingent. I can easily get fuel
that passes the wash test with flying colours but still gives some
precipitate from the methanol test.
BTW out of curiosityhow many of you get zero precipitate in the
methanol test? Can we have a show of hands?

Joe


JJJN wrote:

  Thanks Jan,
You have confirmed what I have researched from JtF about the base 
converting the methyl esters back to mono and di glycerides (can happen) 
and that certainly makes sense as the bio was unwashed therefore it 
would have had additional catalyst available for this to happen.

Thanks again for your help here

Jan Warnqvist wrote:

  
  
Hello Jim,
since the methanol solubility test worked out well, you probably have
created some soap from the methyl esters.
With best regards
Jan
Jan Warnqvist
AGERATEC AB

[EMAIL PROTECTED]

+ 46 554 201 89
+46 70 499 38 45
- Original Message - 
From: "JJJN" [EMAIL PROTECTED]
To: "BIO" Biofuel@sustainablelists.org
Sent: Monday, January 02, 2006 7:32 PM
Subject: [Biofuel] Biodiesel Testing excessive methanol


 



  I just tested a 60 Liter batch and have a few questions; below is what I
have done with the results and further below are my questions,

The biodiesel used in the tests below was unwashed - glycerin layer
removed.

1.) Using the test method noted on JtF ( Jan Warnqvist - Methanol test)
as prescribed 225 ml Methanol combined with 25 ml of the biodiesel.
Results: Biodiesel was fully soluble and formed a clear bright phase no
contaminants or other phases noted. Results after 24 hours - No change.

2) Using a MODIFIED JtF method,  (combining 4.90875 grams lab grade KOH
and 100 ml Methanol (Potassium Methoxil) with 1 Liter of the biodiesel)
- INSTEAD I added 400ml methanol and 4.90875 grams KOH ( Potassium
Methoxil ) (both lab grade near absolute) to 1 Liter of the Biodiesel. I
then heated to 120 deg F and mixed for one hour.
Results: after 24 hours  there was a nice amber layer from the bottom of
the glass jar up to the last say 1/2 inch where a very very slightly
amber layer resided to the top. there was nothing at the bottom at all.

3) Wash test JtF, In a glass jar I shook 1/2 Bio and 1/2 water at room
temp till mixed into one phase.
Results: within 1 minute the water and Bio separated and the water was
quite white. Wash #2 same time of separation water clearer this time.
Wash # 3 same as #2. Wash # 4 water was not drinking quality but PH is
close to seven.

O.K why did I increase the Methanol in test #2) above?  I am not sure
except to see what it would do, but from what I read it would not harm
so I did.

My Question: Can anyone tell me what the strange clear amber layer on
top of the other clear amber layer may be?

Could this be the FFA content per L?

Thanks in advance,

Jim

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[Biofuel] Geeky process question

2006-01-09 Thread Joe Street
Hi Bob;

I notice you are very sharp on the chemistry so I have a question for 
you regarding the biodiesel process. Copying to list as well.  I am 
wondering if in these processes where you have two phases that separate 
does the separation proceed over time by an exponential decay?  I mean 
if I measured the amount of say glycerine that comes out per unit of 
time would it be described by a function something like Y= X(1-e^-t/tc) 
where Y would be the amount of glycerine at a given time, X is the total 
amount which will ever settle out, t is the time interval and tc some 
time constant for the reaction conditions?  If this IS the case then 
what factors would dictate tc??  Where I am going with this is that in 
electronics we use this formula to describe the charging of a 
capacitor.  Basically after a period of time equal to five time 
constants there is already 99% of the maximum you will ever get in the 
capacitor.  I am trying to determine a cutoff point for settling in 
order to optimize the process in terms of time, without raising 
contamination levels in the final product unduely.  Am I on the right 
track here?  Sorry but I am not trained in chemistry.

Joe


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Re: [Biofuel] Geeky process question

2006-01-09 Thread Fred Finch
Say Joe, Wouldn't be appropraite if you put Bob Allen - Geeky process question in the heading? fredOn 1/9/06, 
Joe Street [EMAIL PROTECTED] wrote:
Hi Bob;I notice you are very sharp on the chemistry so I have a question foryou regarding the biodiesel process. Copying to list as well.I amwondering if in these processes where you have two phases that separate
does the separation proceed over time by an exponential decay?I meanif I measured the amount of say glycerine that comes out per unit oftime would it be described by a function something like Y= X(1-e^-t/tc)
where Y would be the amount of glycerine at a given time, X is the totalamount which will ever settle out, t is the time interval and tc sometime constant for the reaction conditions?If this IS the case then
what factors would dictate tc??Where I am going with this is that inelectronics we use this formula to describe the charging of acapacitor.Basically after a period of time equal to five timeconstants there is already 99% of the maximum you will ever get in the
capacitor.I am trying to determine a cutoff point for settling inorder to optimize the process in terms of time, without raisingcontamination levels in the final product unduely.Am I on the righttrack here?Sorry but I am not trained in chemistry.
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Re: [Biofuel] Geeky process question

2006-01-09 Thread bob allen
Howdy Joe,

to be honest I have never given thought to the kinetics of phase separation, 
although your intuitive 
guess at an exponential rate for the process certainly seems reasonable.  
Variables would include 
viscosities of both phases, the difference in densities of the phases, and 
maybe the  difference in 
the polarities of the phases, and I would bet most importantly, temperature.  
The variables are not 
completely independent as viscosity is a function of temperature, even the 
densities may vary 
differently as a function of temperature. Further, unless you have essentially 
infinite partition 
coefficients, you will always have some of each dissolved in the other.  and 
one more thing, the two 
phases are not homogeneous, the glycerin phase also contains the unreacted 
methanol, and alkaline 
catalyst, small amounts of mono and diglycerides, etc.

If I were to approach the problem, I would certainly do it empirically.  take 
crude reaction mixture 
after it had cooled to room temperature (to control for temperature which is an 
important variable), 
remix it, then put it in a burette, and monitor phase separation over time.


All that having been said, does it really matter that much, considering that 
good washing will 
remove any of the glycerin cocktail not separated by gravity?



   Hi Bob;
 
 I notice you are very sharp on the chemistry so I have a question for
 you regarding the biodiesel process. Copying to list as well.  I am
 wondering if in these processes where you have two phases that separate
 does the separation proceed over time by an exponential decay?  I mean
 if I measured the amount of say glycerine that comes out per unit of
 time would it be described by a function something like Y= X(1-e^-t/tc)
 where Y would be the amount of glycerine at a given time, X is the total
 amount which will ever settle out, t is the time interval and tc some
 time constant for the reaction conditions?  If this IS the case then
 what factors would dictate tc??  Where I am going with this is that in
 electronics we use this formula to describe the charging of a
 capacitor.  Basically after a period of time equal to five time
 constants there is already 99% of the maximum you will ever get in the
 capacitor.  I am trying to determine a cutoff point for settling in
 order to optimize the process in terms of time, without raising
 contamination levels in the final product unduely.  Am I on the right
 track here?  Sorry but I am not trained in chemistry.
 


-- 
Bob Allen
http://ozarker.org/bob

Science is what we have learned about how to keep
from fooling ourselves - Richard Feynman

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[Biofuel] Fwd: [PasturedPigs] NAIS letter

2006-01-09 Thread Garth Kim Travis
Greetings,
Please call your representatives, senators and everyone you can.  This bill 
includes cats and dogs.  And if you think it is about preventing disease, 
think about this:  All of your food will be microchiped!  I do know how 
hard it is to find those microchips and remove them when you butcher, the 
emu industry used them.  We could all wind up with a pound of microchips in 
our intestines.
Bright Blessings,
Kim



Worth reading. Worth thinking about. Worth writing about. Worth
fighting.

Begin forwarded message:

From: Laura Haggarty [EMAIL PROTECTED]
Date: January 9, 2006 9:39:31 AM EST

Hi all,

I got this letter from another email list (with permission to cross-post
and use), made a few small modifications, and have sent it to my local
newspaper (have already written to my legislators.) I thought you all
might want to send it along to yours:

   Dear Editors,

I am writing to ask the Grant County News to publish my letter in order
to inform their subscribers about the National Animal Identification
System (NAIS) which is currently in its initial stages. This USDA-run
program has as its goal the registration of every farm animal (including
non-food animals such as horses) in a centralized government database.
This program will require micro chipping of each animal (including all
forms of poultry), at the expense of the owner, and a premises ID for
every farm which will be linked to a satellite photo and Global
Positioning System record (see this link for the USDA website about the
program: www.usda.gov/nais/)

As a hobby farm owner who has horses, goats, and poultry, I strongly
oppose the implementation of the NAIS. Agribusiness, specifically The
National Institute for Animal Agriculture (NIAA), lobbied the USDA
(after 9/11 and subsequent BSE scares) to create the NAIS supposedly to
protect U.S. citizens and their animals from diseases. The NIAA is
composed primarily of two groups - (1) large corporate producers and (2)
the makers and producers of animal ID equipment. In April 2002 a task
force composed of the Animal and Plant Health Inspection Service (APHIS)
and over 30 livestock organizations provided leadership in creating the
animal identification system. Small-scale farmers involved in animal
husbandry, homesteaders, and animal hobbyists were not represented.

Language quoted from the Draft Strategic Plan proves this, APHIS then
established the National Identification Development Team (NIDT), a
joint, State, Federal, and industry group to further advance this
effort. Throughout 2003, the NIDT, consisting of approximately 100
animal and livestock industry professionals representing more than 70
associations, organizations, and government agencies, expanded upon the
work plan to produce the initial draft of the U.S. Animal Identification
Plan (USAIP). (Plan, p. 4) While associations, organizations, etc. may
be backing the NAIS, they did not inform their members of this proposed
legislation. Chances are the members still have no idea that their
freedoms are being given away.

   I am writing in opposition of the National Animal Identification
System
because:

   (1) Should the NAIS become law, we will be forced to pay fees to
register our farms and animals. Even with public funding, there will be
costs to producers. (Plan, p. 11)
   (2) We will be forced to report to the national animal records
repository within a short-term specified timeframe the birth, death, and
loss of identification device, sale, or movement of any animal in our
possession.
   (3) We will be required to report to the national animal records
repository when an animal we own attends a livestock show, participates
in a trail ride, is transported to another farm for stud service, or
takes part in a community parade, etc.
   (4) Our personal information collected through NAIS could be disclosed
- the USDA cannot assure the confidentiality of all the information at
the present time. (Plan, p. 15) Financial institutions were not able to
keep this information confidential, so it is no surprise that USDA
cannot guarantee confidentiality.
   (5) The NAIS will violate the religious beliefs of minority faith
communities by requiring them to become part of this computerized,
technology-dependent system or abandon the livestock ownership necessary
for their way of life. (Many adherents raise their own food animals and
use animals in farming and for transportation. Some, by scriptural
teaching, would refuse to take the mark of such a numbering system.)
   (6) Our livestock would become part of the national herd. (Plan, p.
8)

Not only would small farm operators be negatively affected by the NAIS,
but this legislation will do serious damage to feed store owners, farm
supply houses, hatcheries that sell and ship day-old poultry, and other
businesses frequented by farmers.

The most common types of meat contamination in the U.S. are the
occurrences of pathogens such as Listeria or E. Coli in processed meat.
When meat becomes 

Re: [Biofuel] Fwd: [PasturedPigs] NAIS letter

2006-01-09 Thread Michael Redler
That only falls in line with other policies in the bizzarro world of the federal gubmint:"Clear Skies" initiative that rolls back progress of the clean air actUSA Patriot act that rolls back protection and rights under the constitutionAn unqualified FEMA director who's emails included quotes like "can I quit now?" after Katrina....etc, etc, etc.Why not have a myopic USDA spenda boat loadof dollars tracking thesymptoms rather than theroot cause which, by enlarge, is already known....so what's wrong with feeding livestock the brains and end-trails of their brothers, sisters, cousins and parents anyway?Even if every person on Earth voices dissent against what theUS gubmint is doing, there is still the monumental task of
 picking a priority and direction. I don't see an end in sight unless everycitizenof every country becomes active and voices their dissent.It's everybody's problem.I just get extremely frustrated trying to figure out how much I can do in betweenanti-racistdemonstrations,fighting for quality K-12 education and programs that promote science and engineering - causes that I've adoptedover the last two years.Thank you. Keep up the good work.By the way, there is no point. I'm venting.Mike  Garth  Kim Travis [EMAIL PROTECTED] wrote:  Greetings,Please call your representatives, senators and everyone you can. This bill
 includes cats and dogs. And if you think it is about preventing disease, think about this: All of your food will be microchiped! I do know how hard it is to find those microchips and remove them when you butcher, the emu industry used them. We could all wind up with a pound of microchips in our intestines.Bright Blessings,KimWorth reading. Worth thinking about. Worth writing about. Worthfighting.Begin forwarded message:From: "Laura Haggarty" <[EMAIL PROTECTED]>Date: January 9, 2006 9:39:31 AM ESTHi all,I got this letter from another email list (with permission to cross-postand use), made a few small modifications, and have sent it to my localnewspaper (have already written to my legislators.) I thought you allmight want to send it along to yours: Dear Editors,I am writing to ask the Grant County News
 to publish my letter in orderto inform their subscribers about the National Animal IdentificationSystem (NAIS) which is currently in its initial stages. This USDA-runprogram has as its goal the registration of every farm animal (includingnon-food animals such as horses) in a centralized government database.This program will require micro chipping of each animal (including allforms of poultry), at the expense of the owner, and a premises ID forevery farm which will be linked to a satellite photo and GlobalPositioning System record (see this link for the USDA website about theprogram: www.usda.gov/nais/)[snip]___
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